Pharmaceutical Consultant
Hạn nộp hồ sơ: 03/12/2026 (Còn 25 ngày)
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Mô tả công việc
An international consulting company providing Marketing Authorization and Consultancy in services across regulatory affairs, pharmacovigilance, quality assurance, engineering, validation, technology transfer, project management, GMP compliance services ETC., to the Pharmaceutical and Biotechnology industry, is currently recruiting for a Pharmaceutical Consultant in RA/QA/PV (Junior-mid level)
Regulatory Affairs, Quality Assurance, Pharmacovigilance.
Therapeutic Drugs, Biotech, Medical Device, Cosmetics, Health Food
Location & Work Arrangement:
Hybrid work arrangement, work from office Tuesday to Thursday, location at Ben Thanh Ward, Ho Chi Minh
Responsibilities:
Regulatory Affairs :
Knowledge and familiarity in Medical Device and Drugs registration and life cycle management, cover end to end all aspects regulatory projects for the market, strategize and provide solutions to clients in product registration by providing regulatory support and intelligence, review for compliance, translation, submission of dossier to health authority locally or regionally, and following up on post-approval commitments, variations, change notifications ETC.
Pharmacovigilance:
Local qualified person for Pharmacovigilance reporting and support other PV in the region, where
needed
Quality Assurance:
Support Quality Management System of Good Distribution / Storage and Supply Practices for
Marketing Authorization Holding.
Project management:
Be involved with business development and execution of projects related to regulatory affairs,
Pharmacovigilance and quality assurance with a thorough understanding of regulations and industry
practices, open to any scope that may come by in the pharmaceutical Consulting service industry.
Supporting Functions:
Open to new challenges and new scopes including general management and marketing of the business.
Consultant may be tasked with company administrative matters, which involves marketing, branding and business development, managing client and vendors database, organizing / communication on training events ETC.
Ability of Consultant to demonstrate interest and initiative in this area for the general process improvement and growth of company will be welcome.
List is not exhaustive and varies with consulting opportunities with lots of growth potential for a challenging and rewarding consulting career.
Please submit your resume to [protected info] with current salary, benefits, and earliest date of availability.
Resumes to indicate an experience summary table of product classifications handled, dosage forms, product names if applicable, countries covered.
We regret that only qualified applicants will be contacted.
Regulatory Affairs, Quality Assurance, Pharmacovigilance.
Therapeutic Drugs, Biotech, Medical Device, Cosmetics, Health Food
Location & Work Arrangement:
Hybrid work arrangement, work from office Tuesday to Thursday, location at Ben Thanh Ward, Ho Chi Minh
Responsibilities:
Regulatory Affairs :
Knowledge and familiarity in Medical Device and Drugs registration and life cycle management, cover end to end all aspects regulatory projects for the market, strategize and provide solutions to clients in product registration by providing regulatory support and intelligence, review for compliance, translation, submission of dossier to health authority locally or regionally, and following up on post-approval commitments, variations, change notifications ETC.
Pharmacovigilance:
Local qualified person for Pharmacovigilance reporting and support other PV in the region, where
needed
Quality Assurance:
Support Quality Management System of Good Distribution / Storage and Supply Practices for
Marketing Authorization Holding.
Project management:
Be involved with business development and execution of projects related to regulatory affairs,
Pharmacovigilance and quality assurance with a thorough understanding of regulations and industry
practices, open to any scope that may come by in the pharmaceutical Consulting service industry.
Supporting Functions:
Open to new challenges and new scopes including general management and marketing of the business.
Consultant may be tasked with company administrative matters, which involves marketing, branding and business development, managing client and vendors database, organizing / communication on training events ETC.
Ability of Consultant to demonstrate interest and initiative in this area for the general process improvement and growth of company will be welcome.
List is not exhaustive and varies with consulting opportunities with lots of growth potential for a challenging and rewarding consulting career.
Please submit your resume to [protected info] with current salary, benefits, and earliest date of availability.
Resumes to indicate an experience summary table of product classifications handled, dosage forms, product names if applicable, countries covered.
We regret that only qualified applicants will be contacted.
Yêu cầu
Qualifications:
Bachelor's Degree in Pharmacy or related field.
Candidate should have minimum 1 - 2 years of experience doing regulatory affairs, product registration and submissions to the regulatory authorities, pharmacovigilance, Quality system maintenance.
Preference for experience from Distribution companies importing foreign pharmaceutical products.
Entrepreneurial, problem solver, self-driven, mature, able to work independently or in dynamic environments.
Able to manage projects to completion within allocated timeline.
Be resourceful and able to seek answers to challenging questions regarding the Asian Regulatory environment.
Fluency in business English + native language is required, including both spoken and written with international experience
Experienced with commercial regulatory affairs, in classification ranging from pharmaceuticals, biologics, cosmetics, health food, medical devices, hazardous chemicals ETC.
Availability from Dec 1 onwards
Bachelor's Degree in Pharmacy or related field.
Candidate should have minimum 1 - 2 years of experience doing regulatory affairs, product registration and submissions to the regulatory authorities, pharmacovigilance, Quality system maintenance.
Preference for experience from Distribution companies importing foreign pharmaceutical products.
Entrepreneurial, problem solver, self-driven, mature, able to work independently or in dynamic environments.
Able to manage projects to completion within allocated timeline.
Be resourceful and able to seek answers to challenging questions regarding the Asian Regulatory environment.
Fluency in business English + native language is required, including both spoken and written with international experience
Experienced with commercial regulatory affairs, in classification ranging from pharmaceuticals, biologics, cosmetics, health food, medical devices, hazardous chemicals ETC.
Availability from Dec 1 onwards
Quyền lợi
We offer full time / project base / part time / hybrid flexible working conditions, where candidate may work remotely or on-site at client's office. However, candidate must be able to manage projects to completion within timeline given.
Thông tin khác
Địa điểm làm việc
TP.HCM:Ben Thanh Ward, Ho Chi Minh, Phường Bến Thành (Quận 1, TP.HCM cũ)
TP.HCM:Ben Thanh Ward, Ho Chi Minh, Phường Bến Thành (Quận 1, TP.HCM cũ)
Thông tin chung
- Thu nhập: 20 - 22 triệu
Việc làm tương tự khác
Công ty TNHH Dịch vụ và Kỹ thuật Năng lượng PECC2 - PESE
Hồ Chí Minh, Đồng Nai
10 - 16 triệu VND
CÔNG TY TNHH ĐẦU TƯ VÀ PHÁT TRIỂN VẠN MỸ KHÁNH
Hồ Chí Minh, An Giang
18 triệu - 20 triệu VND
Công ty Cổ phần Giáo dục Toàn Cầu IEG
Hồ Chí Minh
2000000 VND
Công ty Cổ phần đầu tư tona
Hồ Chí Minh
Thỏa thuận cạnh tranh theo năng lực và kinh nghiệm
CÔNG TY TNHH CỬA PHÚ MỸ HƯNG
Hồ Chí Minh
15.000.000 - 20.000.000 VND
Văn phòng đại diện PE PHARMA PTE.LTD. tại thành phố Hà Nội
Xem trang công ty- Địa chỉ công ty: 1 Commonwealth Lane, #07-12, One Commonwealth, Singapore 149544. được thành lập Văn phòng đại diện tại thành phố Hà Nội Điều 2. Tên Văn phòng đại diện
Thông tin công việc
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